Nanoink composition

ABSTRACT

Disclosed is a nanoink composition which can impart electrical conductivity to a surface-protecting ligand layer of an inorganic nanoparticle and does not require any post-treatment such as the removal of ligands. Specifically disclosed is a nanoink composition comprising inorganic nanoparticles ( 1 ) and an organic π-conjugated ligand ( 3 ), and characterized in that the organic π-conjugated ligand ( 3 ) is bound to the inorganic nanoparticles ( 1 ) via π-conjugation to exhibit electrical conductivity.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a Continuation application of U.S. patentapplication Ser. No. 13/634,565 which is a national-stage applicationunder 35 U.S.C. 371 of PCT application No. PCT/JP2011/001509 filed onMar. 15, 2011, and claims priority of the application entitled “NANOINKCOMPOSITION” filed with the Japan Patent Office on Mar. 15, 2010, andassigned Patent Application No. 2010-056840, the entire contents of eachof which are incorporated herein by reference.

TECHNICAL FIELD

The present invention relates to a nanoink composition.

BACKGROUND ART

An integrated electronic circuit as a typical semiconductor is improvedin the function by increasing the integration density. Thus, amanufacturing method of forming a conductive circuit in a vacuum withthe sputtering or the vapor deposition has been adopted. Since it is apremise that the process is conducted in the vacuum, an apparatusthereof is expensive and a huge investment is required to shift a nextgeneration of higher integration density. An enormous energy is alsorequired in order to keep the vacuum condition. Therefore, a conductivenanoink necessary for forming the conductive circuit in an ink-jet typeat normal temperature and at normal pressure.

Inorganic nanoparticles have been widely utilized in a conductivenanoink (e.g., see Patent Reference 1 and the like). Organic ligandsprotecting surfaces of the inorganic nanoparticles are indispensable inorder to keep the inorganic nanoparticles staying stably in the nanoink.Since the organic ligand is electrically insulating, a thin coating filmobtained by applying and drying nanoink of a nanoparticle solution isalso electrically insulating. Conventionally, it was necessary to removeligands by the post-treatment with chemicals and by firing at hightemperature in order to convert it from electrically insulative toconductive. In such processing, there was limitation in selection of asubstrate (e.g., see Non-patent Reference 1 and the like).

On the other hand, the present inventors investigated organic ligandsand gold particles and presented a paper that characteristic opticalproperties were expressed with pi junction (e.g., see Non-patentReference 2 and the like).

PRIOR ART TECHNOLOGY Patent Reference

-   Patent Reference 1: JP A 2009-295965

Non-Patent Reference

-   Non-Patent Reference 1: Matt, Law and five others, “Structural,    Optical, and Electrical Properties of Pb Se Nano crystal Solids    Treated Thermally or with Simple Amines,” J. Am. Chem. Soc. 2008,    130 5974-5985.-   Non-Patent Reference 2: Masayuki, Kanehar, and two others, “Gold(0)    Prophyrins on Gold Nanoparticles,” Angew. Chem. Int. Ed. 2008, 47,    307-309.

SUMMARY OF THE INVENTION Problems to be Resolved by the Invention

In order to keep thermodynamically unstable inorganic nanoparticlesstaying in a stable condition for a long period of time, ligands areindispensable and organic ligands having long-chain alkyl groups such asdecanethiol have been conventionally utilized. However, in a case whereligand layers are made of octanethiol with respect to these sigma-typeligands, nanoink has a value of resistance as large as several gigas ofohms just as applied. Therefore, with respect to the nanoink having suchligand layers, it was necessary to remove these ligand layers of highresistance after application. It has been assumed that it is verydifficult to realize a nanoink composition in which electricalconductivity is imparted to surface-protecting ligand layers ofinorganic nanoparticles such that the post-treatment such as removal ofligands is not necessary (see (1) Talapin, D. V; Murray, C. B. Science2005, 310, 86-89 (page 8) or (2) Law, M.

Luther, J. M. Song, Q. Hughes, B. K.; Perkins, C. L.; Nozik, A. J. J.Am. Chem. Soc. 2008, 130, 5974-5985 (pages 5974 and 5975)).

It is an object of the present invention to provide a nanoinkcomposition in which electrical conductivity is imparted tosurface-protecting ligand layers of inorganic nanoparticles such thatthe post-treatment such as removal of ligands is not necessary.

Means of Solving the Problems

The present inventors intensively conducted the research and developmentin order to resolve the above problems. In particular, effects ofstrength of pi junction (n junction) and steric hindrance betweenparticles on the electrical conductivity have been investigated. As aresult, meaning that pi junction organic ligands are connected to metalnanoparticles with pi junction was found so as to complete the presentinvention.

(1) A nanoink composition comprising: an inorganic nanoparticle, anorganic pi conjugated ligand, and a solvent, wherein the organic piconjugated ligand is connected to the inorganic nanoparticle withpi-junction such that electrical conductivity is caused by strongpi-junction and access among particles.

The nanoink composition of the present invention as described in (1) hasan electrical conductive property as the organic pi conjugated ligand isconnected to the inorganic nanoparticle with pi junction. Here, the pijunction is that pi conjugate plane of pi conjugated molecule is joinedin parallel to a surface of the inorganic nanoparticle. And the organicpi conjugated ligand is an organic ligand to make such pi junctioneffective to the inorganic nanoparticle.

FIG. 1 is a diagram illustrating a concept of the nanoink compositionaccording to the present invention. Conventionally, an inorganicnanoparticle 1 has to have a ligand in order to keep the thermallyunstable inorganic nanoparticle in a stable condition for a long periodof time as shown in FIG. 1 (a) and conventionally an organic ligandhaving a long alkyl group such as decanethiol and the like is mainlyused. However, these sigma type ligands 2 have a long insulating organicstructural portion such that a ligand layer has a large value ofresistance and the value of resistance was about several gigas of ohm(Ω) in the case where the sigma type ligand is octanethiol.

In the nanoink composition according to the present invention, as shownin FIG. 1(b), the organic pi conjugated ligand 3 is connected with pijunction. With respect to the organic pi conjugated ligand 3 as shown inFIG. 1 (b), the ligand layer is thin and pi orbital is positioned in anadvantageous direction for the electrical conductance between particlessuch that the resistance of the ligand layer is relatively low and anelectrical conductive property is expressed at the organic pi conjugatedligand 3 due to mutual interaction of orbital of the inorganicnanoparticle by the pi junction. Therefore, the nanoink compositionaccording to the present invention has the electrical conductiveproperty.

The pi junction is a strong mutual interaction between the organic piorbital—the inorganic nanoparticle orbital created by bringing theorganic pi orbital close to the surface of the inorganic nanoparticle.The strength of the pi junction can be quantitatively evaluated by theultraviolet-visible light spectral measurement. Porphyrin andphthalocyanine have characteristic absorbance as referred to as soretband and Q band in the visible light range. When the strong pi junctionis expressed, the organic pi orbital is metalized by the strong mutualinteraction between the organic and the inorganic such that the abovecharacteristic absorbance becomes significantly broadened. In order toobtain the conductive nanoparticle, the strong pi junction and approachof particles are necessary.

(2) The nanoink composition as described in (1), wherein the organic piconjugated ligand is an organic pi conjugated ligand which has one ormore of substituent groups of amino group, mercapto group, hydroxylgroup, carboxyl group, phosphine group, phosphonate group, halogengroup, selenol group, sulfide group, and seleno ether group, the one ormore of substituent groups coordinating to a surface of the inorganicnanoparticle.

(3) The nanoink composition as described in (1), wherein the organic piconjugated ligand is an organic pi conjugated ligand which has one ormore of substituent groups of hydroxyl group, carboxyl group, aminogroup, alkylamino group, amido group, imide group, phosphonate group,sulfonate group, cyano group, nitro group, and salt thereof, the one ormore of substituent groups enabling the inorganic nanoparticle beingsoluble to a solvent containing water and an alcohol solvent.

(4) The nanoink composition as described in any one of (1) to (3),wherein the solvent is water or a solvent mixed with water, or alcoholor a solvent mixed with alcohol.

Since water, a solvent mixed with water, or alcohol or a solvent mixedwith alcohol are low in the cost and easy to handle. Here, theconstituent other than water can be alcohol, ether, ketone, amido, etc.and it is preferable to be alcohol and the like, more preferable to bealcohol and the like having on to 10 carbons. More specifically, as asolvent of alcohol system, methanol, ethanol, n-propanol, isopropanol,n-butanol, isobutanol, 2-butanol, tert-butanol, 1-pentanol,2-methyl-1-butanol, isoamyl alcohol, hexyl alcohol, heptyl alcohol,octyl alcohol, capryl alcohol, nonyl alcohol, decyl alcohol, undecylalcohol, lauryl alcohol, allyl alcohol, crotyl alcohol, propargylalcohol, cyclopentanol, cyclohexanol, 2-methoxyethanol, 2-ethoxyethanol,2-butoxyethanol, ethylene glycol, propylene glycol ye, etc. can becited. Among these solvents, as particularly preferable solvent,methanol, ethanol, 2-ethoxyethanol, ethylene glycol, and propyleneglycol can be used.

(5) The nanoink composition as described in any one of (1) to (3),wherein the inorganic nanoparticle is made of one metal, a mixture oftwo or more metals, or an alloy with two or more metals of gold, silver,copper, platinum, palladium, nickel, ruthenium, indium, and rhodium.

(6) The nanoink composition as described in any one of (1) to (3),wherein the inorganic nanoparticle is either semiconductor particle orelectro-conductive oxide particle.

In the nano ink composition according to the present invention asdescribed in (6), as the inorganic nanoparticle, a semiconductorparticle or an electrical conductive oxide particle is used. Thesemiconductor particle and the electrical conductive oxide particlecomprises what exhibits special properties of various kinds and it ispossible to expect new applications by protecting such specialproperties by the organic pi conjugated ligand.

(7) The nanoink composition as describe in (1), wherein the organic piconjugated ligand is OTAP.

Here, OTAP is academically called as “2, 3, 9, 10, 16, 17, 23,24-octakis [(2-N, N-dimethylamino ethyl) thio] phthalocyanine”(hereinafter referred to as “OTAP”) and is an organic pi conjugatedligand having a chemical structure as shown in FIG. 3.

(8) The nanoink composition as describe in (1), wherein the organic piconjugated ligand is OTAN.

Here, OTAN is called as “2, 3, 11, 12, 20, 21, 29, 30-octakis [(2-N,N-dimethylamino ethyl) thio] naphthalocyanine (hereinafter referred toas “OTAN”) and is an organic pi conjugated ligand having a chemicalstructure as shown in FIG. 6.

(9) A manufacturing method of a nanoink composition comprising the stepsof: a gold nanoparticle production step in which an aqueous solution ofchlorauric acid is boiled and trisodium citrate is quickly added theretoas being stirred vigorously and a mixture thereof is boiled such that acitrate protecting gold nanoparticle solution is produced; and a step inwhich OTAP formate is added to the citrate protecting gold nanoparticlesolution such that phthalocyanine 3 protecting gold nanoparticle isproduced.

According to the manufacturing method of the nanoink composition of thepresent invention as described in (7), the gold nanoink composition ofthe present invention can be manufactured.

(10) A manufacturing method of a nanoink composition comprising thesteps of: a gold nanoparticle production step in which an aqueoussolution of chlorauric acid is boiled and trisodium citrate is addedthereto as being stirred vigorously and a mixture thereof is boiled suchthat a citrate protecting gold nanoparticle solution is produced; and astep in which OTAN formate is added to the citrate protecting goldnanoparticle solution such that phthalocyanine 3 protecting goldnanoparticle is produced.

According to the manufacturing method of the nanoink composition of thepresent invention as described in (10), the gold nanoink composition ofthe present invention can be manufactured.

Effects of the Invention

According to the present invention, it is possible to provide a nanoinkcomposition and a manufacturing method thereof wherein the nanoinkcomposition does not require the post-treatment to remove ligands as thesimply applied and dried nanoink composition at normal temperature andin normal pressure has an electrical conductive property while thesurface protecting ligand layer, which is conventionally an electricallyinsulating layer, becomes imparted with electrically conductiveproperties.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a diagram illustrating a concept of a nanoink compositionaccording to the present invention.

FIG. 2 is a diagram illustrating a concept of a nanoink compositionhaving a pi junction organic ligand according to the present invention.

FIG. 3 is a chemical structure diagram of OTAP asapi junction organicligand utilized in a nanoink composition according to the presentinvention.

FIG. 4 is a diagram illustrating manufacturing processes of OTAP as a pijunction organic ligand utilized in a nanoink composition according tothe present invention.

FIG. 5 is a transmission electron microscope image of an OTAP protectinggold nanoparticle nanoink composition according to the presentinvention.

FIG. 6 is a chemical structure diagram of pi junction organic ligandOTAN of another embodiment according to the present invention.

FIG. 7 is a diagram illustrating a manufacturing method of pi junctionorganic ligand OTAN utilized in a nanoink composition according to thepresent invention.

FIG. 8 shows UV-vis spectra of OTAP and OTAN.

FIG. 9 shows UV-vis spectra of OTAP and OTAN protecting goldnanoparticles.

FIG. 10 is a diagram illustrating a concept of a nanoink compositionhaving pi junction organic ligands according to the present invention.

FIG. 11 shows UV-vis spectra of OTAP protectingpalladium-core-gold-shell nanoparticles.

FIG. 12 is a chemical structure diagram of 1, 8, 15, 22-tetrakis[(2-N,N-dimethylaminoethyl) thio] phthalocyanine of pi junction organic ligandof another embodiment according to the present invention.

FIG. 13 is a chemical structure diagram of SC0P.

FIG. 14 is a chemical structure diagram of SC1P.

FIG. 15 shows UV-vis spectra of SCnP ligand (inserted diagram shows10-times enlarged spectra in Q band).

FIG. 16 shows UV-vis spectra of SCnP ligand protecting goldnanoparticles.

FIG. 17 is a model diagram of coordination structure of coordination ona gold nanoparticle of SC0P.

FIG. 18 is a model diagram of coordination structure of coordination ona gold nanoparticle of SC1P molecule.

FIG. 19 is a chemical structure diagram of SPc.

FIG. 20 shows a TEM image of SPc protecting gold nanoparticles.

FIG. 21 shows UV-vis spectra of SPc and SPc protecting goldnanoparticles.

MODE FOR CARRYING OUT THE INVENTION

In the following, an embodiment of the present invention will beexplained with reference to the drawings. Here, this is explained as anexample and the technical scope of the present invention is not limitedto this.

Embodiment 1

Embodiment 1 is an example in which gold was used for inorganicparticles and OTAP was used for pi junction organic ligands.

Embodiment 1

FIG. 2 is a diagram illustrating a concept of a nanoink compositionaccording to the present invention. As shown in FIG. 2, an inorganicparticle 1 is made of gold and a pi junction organic ligand 3 is made ofOTAP. As shown in FIG. 2, the pi junction organic ligand 3 of OTAPstrongly adheres to the inorganic particle 1 of gold.

In reference to FIG. 3, a manufacturing method of manufacturing ananoink composition utilizing OTAP according to the present invention.

(Manufacturing Method of OTAP Organic Pi-Conjugated Ligand)

As shown in FIG. 4, synthesis of 4, 5-bis[(2-N, N-dimethylaminoethyl)thio] phthalonitrile (FIG. 4-2) was conducted by dissolving 4,5-dichlorophthalonitrile (FIG. 4-1, 5.0 g, 25 mmoL) and N,N-dimethylaminoetanethiolhydorochloride (9.0 g, 64 mmoL) with dehydratedDMF (100 mL), dripping dehydrated diisopropylethylamine (14 mL, 80 mmoL)thereinto, and stirring them at room temperature for four hours. After200 mL of water was added to the solution and organic material wasprecipitated, the mixture solution was filtrated and then purified withcolumn chromatography alumina (dichloromethane/ethyl acetate=2/1) suchthat 4, 5-bis [(2-N, N-dimethylaminoethyl) thio] phthalonitrile (FIG.4-2, 23.0 g, 29% was obtained.

Synthesis of (2, 3, 9, 10, 16, 17, 23, 24-octakis [(2-N,N-dimethylaminoethyl) thio] phthalocyanine, OTAP) was conducted byadding 4, 5-bis [(2-N, N-dimethylaminoethyl) thio] phthalonitrile (FIG.4-2, 1.7 g, 5.0 mmoL) to a solution in which lithium (0.35 g, 50 mmoL)was dissolved with n-pentanol (30 mL) and conducting reflux thereof for12 hours. The solvent was distilled away and the rest was washed withwater and acetonitrile such that 2, 3, 9, 10, 16, 17, 23, 24-octakis[(2-N, N-dimethylaminoethyl) thio] phthalocyanine (OTAP, 1.1 g, 65%) wasobtained.

(Synthesis of OTAP Protecting Pi Junction Gold Nanoparticles)

An aqueous solution of chlorauric acid (1 mM, 2 L) was boiled andtrisodium citrate (1M, 4 mL) was quickly added thereto as being stirredvigorously and the mixture was boiled for 30 minutes such that a citrateprotecting gold nanoparticle solution was obtained. OTAP formate (20 mg)was added thereto and the mixture was stirred for 30 minutes. Themixture was purified with water and ethanol and was dissolved with purewater such that an OTAP protecting pi junction gold nanoparticlesolution was obtained. A methanol solution containing 50% of OTAPprotecting pi junction gold nanoparticles was obtained by dissolving themixture with a water/methanol=1/1 solvent.

A transmission electron microscope image of a nanoink composition, whichwas manufactured as described above, in an applied condition is shown inFIG. 5. As shown in FIG. 5, nanoparticles are dispersed such that it wasfound that the nanoink composition was able to be reduced into practice.

Further, the value of resistance between sections 1 cm apart as in anapplied and dried condition at normal temperature was 0.4 Ω. Themeasurement was conducted with Tester KU-1188 manufactured by KAISECORPORATION. Here, the thickness of the film measured was 1 μm.

A thin film of nanoparticles having a uniform thickness with width of 1mm and length of 2 cm was manufactured with an OTAP protecting goldnanoparticle solution. The thin film was subject to a mild heattreatment at 55° C. for 30 minutes in order to evaporate remaining watermolecules completely after it was dried at room temperature. And theelectrical conductivity of this thin film was evaluated by thefour-terminal method (IEC60093, JISK6911) and the electricalconductivity of this OTAP protecting gold nanoparticle was 1560 S/cm.Therefore, it was found to be electrically conductive and of practicaluse.

With respect to OTAP and OTAN protecting gold nanoparticles, Q bands(see FIG. 8) near 650 and 700 nm having been observed when they werejust ligands by themselves almost disappeared (see FIG. 9). Thisindicates existence of a strong pi junction. Since OTAN and OTAP haveeight side chains substituted at beta positions, as conceptually shownin FIG. 10, the side chains do not rise up outward even when thenanoparticles are coordinated to such that particles can getsufficiently close enough. Therefore, the electrical conductivity isexpressed.

Embodiment 2

In Embodiment 2, the organic pi conjugated ligand is made of OTAN andthe inorganic nanoparticle is made of gold.

(Manufacturing Method of OTAN Organic Pi Conjugated Ligand)

As shown in FIG. 7, synthesis of 2, 3-dicyano-6, 7-bis [(2-N,N-dimethylaminoethyl) thio] naphthalene (FIG. 7-4) was conducted bydissolving (2, 3-Dibromo-6, 7-dicyanonaphthalene) (FIG. 7-3, 2.54 g,7.56 mmol) and N, N-dimethylamino ethanethiol hydrochloride (3.21 g,22.7 mmol) with dehydrated DMF (30 mL), dripping 1,8-diazabicyclo[5.4.0]undec-7-ene (6.78 mL, 45.4 mmol) into the solution,and stirring the mixture at room temperature for one hour. Water of 30mL was added to the solution and organic material was precipitated suchthat 2, 3-dicyano-6, 7-bis [(2-N, N-dimethylamino ethyl) thio]naphthalene (FIG. 7-4, 2.50 g, 88%) was obtained.

Synthesis of (2, 3, 11, 12, 20, 21, 29, 30-octakis [(2-N,N-dimethylaminoethyl) thio] naphthalocyanine, OTAN) was conducted, asshown in FIG. 7, by adding 2, 3-dicyano-6, 7-bis [(2-N, N-dimethylaminoethyl) thio] naphthalene (FIG. 7-4, 816 mg, 2.12 mmol) to n-pentanol (30mL) in which lithium (147 mg, 21.2 mmol) was dissolved, and conductingreflux for two hours. Solvent was distilled away and the rest was washedwith water and acetonitrile such that 2, 3, 11, 12, 20, 21, 29,30-octakis [(2-N, N-dimethylamino ethyl) thio] naphthalocyanine, (OTAN,377 mg, 46%) was obtained.

(Manufacturing Method of OTAN Protecting Pi Junction Gold Nanoparticles)

An aqueous solution of chlorauric acid (1 mM, 2 L) was boiled andtrisodium citrate (1M, 4 mL) was quickly added thereto as being stirredvigorously and the mixture was boiled for 30 minutes such that a citrateprotecting gold nanoparticle solution was obtained. OTAN formate (20 mg)was added thereto and the mixture was stirred for 30 minutes. Themixture was purified with water and ethanol and was dissolved with purewater such that an OTAN protecting pi junction gold nanoparticlesolution was obtained.

As explained above, the nano ink composition was manufactured andapplied onto a glass substrate in the same way as with Embodiment 1 suchthat the value of resistance was measured to obtain a value ofresistance such that the value of resistance between sections 1 cm apartwas 0.5Ω at normal temperature as being applied and dried. Here, thethickness of the film measured was 1 μm.

A thin film of nanoparticles having a uniform thickness with width of 1mm and length of 2 cm was manufactured with an OTAN protecting goldnanoparticle solution. The thin film was subject to a mild heattreatment at 55° C. for 30 minutes in order to evaporate remaining watermolecules completely after it was dried at room temperature. Theelectrical conductivity of this thin film was evaluated by thefour-terminal method (IEC60093, JISK6911) and the electricalconductivity of this OTAP protecting gold nanoparticle was 5370 S/cm.

Embodiment 3

Embodiment 3 relates to OTAP protecting pi junctionpalladium-core-gold-shell nanoparticles.

(Manufacturing Method of OTAP Protecting Pi JunctionPalladium-Core-Gold-Shell Nanoparticles)

Aqueous solutions (200 mL) of palladium (II) sodium chloride (0.4 mmol)and lithium citrate (1 mmol) were stirred vigorously in an ice waterbath as an aqueous solution of sodium borohydride (200 mM, 1 mL) wasquickly added thereto, and the mixture was stirred for five minutes suchthat palladium nanoparticles were obtained. An aqueous solution ofsodium disulfitoaurate (I) (500 mM, 0.1 mL) was added thereto and thetemperature was raised up to 50° C. OTAP formate (20 mg) was addedthereto and the mixture was stirred for 10 minutes. The mixture waspurified with water and ethanol and dissolved with pure water such thatan aqueous solution of OTAP protecting pi junctionpalladium-core-gold-shell nanoparticles was obtained.

The result of UV-vis spectral measurement of OTAP protecting pi junctionpalladium-core-gold-shell nanoparticles synthesized as described aboveis shown in FIG. 11. As shown in FIG. 11, the soret band near 420 nm wasbroadened and so much broadening was recognized such that the Q bandfrom 500 to 700 nm could not be observed, thereby expecting there was astrong pi junction.

As described above, the nanoink composition was manufactured and appliedonto a glass substrate in the same way as with Embodiment 1 such thatthe value of resistance was measured to obtain a value of resistancesuch that the value of resistance between sections 1 cm apart was 100Ωat normal temperature as being applied and dried. The thickness of thefilm measured was 1 μm. The value is similar to that of Embodiment 1such that it has been found that it could be put in practical use.

Embodiment 4

In Embodiment 4, the organic pi conjugated ligand is made of 1, 8, 15,22-tetrakis[(2-N, N-dimethylaminoethyl) thio] phthalocyanine as shown inFIG. 12, and the inorganic nanoparticle is made of gold. In the same wasas described with Embodiment 1, the nanoink composition was manufacturedand applied onto a glass substrate such that the value of resistance wasmeasured such that the value of resistance between sections 1 cm apartwas 4×10³Ω at normal temperature as being applied and dried. Here, thethickness of the film measured was 1 μm. It has been found that it couldbe useful depending on the area of application.

It has been found that electrical conductivity is expressed in the casewhere various organic pi conjugated ligands and inorganic nanoparticlesare made of gold or palladium-core-gold-shell as described above.

Comparative Example 1

With the gold nanoparticles having particle diameter of 10 nm andprotected by pi junction porphyrin ligands SCnP of a chemical structureas shown in FIGS. 13 and 14, the soret bands near 420 nm were broadened,as shown in FIGS. 15 and 16, while the soret bands were observed withSCnP alone. When broadening of the soret bands is focused on, broadeningof SC0P coordinated much closer to the surface of the gold nanoparticleis much more significant. However, as shown in FIGS. 17 and 18, strengthof the pi junction of these gold nanoparticles is insufficient andsteric hindrance is caused because four substituting phenyl groups atmeso positions twist with respect to the porphyrin ring such thatparticles cannot get sufficiently close with each other, thereby notexpressing the electrical conductivity.

Comparative Example 2

Much closer coordination to the surface of the nanoparticle was at firstexpected and phthalocyanine derivative SPc protecting gold nanoparticleshaving a chemical structural formula as shown in FIG. 19 were preparedand investigated. A TEM image picture is shown in FIG. 20.

With respect to the phthalocyanine derivative SPc protecting goldnanoparticles (particle diameter: 3 nm), as shown in FIG. 21, Q bandnear 750 nm which is characteristic to phthalocyanine almostdisappeared. This is a result indicating a strong pi junction. However,since SPc has eight hexyl groups at alpha positions, which has astructure with arms extending outward from a particle when the hexylgroups coordinate to the nanoparticle because of steric hindrance ofeach other as a feature of side chains at alpha positions, as a result,it has been found that the electrical conductivity is not expressed withthe SPc protecting gold nanoparticle (Two positions closer to thephthalocyanine base structure are referred to as alpha positions and twoother positions farther from it are referred to as beta positions.).

As mentioned above, it has been explained with examples of the presentinvention, but the technical scope of the present invention is notlimited to that of descriptions of the aforementioned examples. Theaforementioned examples can be subject to various kinds of modificationsor improvements. It is clear that such examples to which various kindsof modifications or improvements are added are included in the technicalscope of the present invention from the description of the claims. Forexample, it has been explained with the case where the inorganicnanoparticle is made of gold, but other inorganic nanoparticles can alsobe applied in the same way.

DESCRIPTION OF NUMERALS

-   1 inorganic nanoparticle-   2 sigma organic ligand-   3 organic pi conjugated ligand

What is claimed is:
 1. A nanoink composition comprising: an inorganicnanoparticle comprising at least one metal, a mixture of at least twometals, or an alloy of at least two metals, wherein the at least onemetal or the at least two metals are selected from a group consisting ofgold, silver, copper, palladium, nickel, ruthenium, indium, and rhodium;an organic pi conjugated ligand comprising: a phthalocyanine ornaphthalocyanine derivative having one or more substituent groupssubstituting at only beta position of phthalocyanine or naphthalocyaninewherein one or more substituent side chains are any one or moresubstituent groups of mercapto group, phosphine group, halogen group,selenol group, sulfide group, and seleno ether group, and/or any one ormore substituent groups of hydroxyl group, carboxyl group, amino group,alkylamino group, amido group, imide group, phosphonate group, sulfonategroup, cyano group, nitro group, and salt thereof; and a solvent,characterized in that a Q band of the phthalocyanine or naphthalocyaninedisappears.
 2. The nanoink composition according to claim 1 wherein thesolvent comprises water or a solvent mixed with water, or alcohol or asolvent mixed with alcohol.
 3. The nanoink composition according toclaim 1 wherein the organic pi conjugated ligand comprises OTAP.
 4. Thenanoink composition according to claim 2 wherein the organic piconjugated ligand comprises OTAP.
 5. The nanoink composition accordingto claim 1 wherein the organic pi conjugated ligand comprises OTAN. 6.The nanoink composition according to claim 2 wherein the organic piconjugated ligand comprises OTAN.
 7. A nanoink composition comprising:an inorganic nanoparticle comprising at least one metal, a mixture of atleast two metals, or an alloy of at least two metals, wherein the atleast one metal or the at least two metals are selected from a groupconsisting of gold, silver, copper, palladium, nickel, ruthenium,indium, and rhodium; an organic pi conjugated ligand comprising: aphthalocyanine or naphthalocyanine derivative having one or moresubstituent groups substituting at only one of two alpha positions ofphthalocyanine or naphthalocyanine wherein one or more substituent sidechains are any one or more substituent groups of mercapto group,phosphine group, halogen group, selenol group, sulfide group, and selenoether group, and/or any one or more substituent groups of hydroxylgroup, carboxyl group, amino group, alkylamino group, amido group, imidegroup, phosphonate group, sulfonate group, cyano group, nitro group, andsalt thereof; and a solvent, characterized in that a Q band of thephthalocyanine or naphthalocyanine disappears.
 8. The nanoinkcomposition according to claim 7 wherein the solvent comprises water ora solvent mixed with water, or alcohol or a solvent mixed with alcohol.9. The nanoink composition according to claim 7 wherein organic piconjugated ligand comprises 1, 8, 15, 22-tetrakis[(2-N,N-dimethylaminoethyl) thio] phthalocyanine.
 10. The nanoink compositionaccording to claim 8 wherein organic pi conjugated ligand comprises 1,8, 15, 22-tetrakis[(2-N, N-dimethylaminoethyl) thio] phthalocyanine.